NDC 70518-3790
Bupropion Hydrochloride(XL) 300 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-145.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA207479
- On the market since
- Jul 13, 2023
- Package NDCs
70518-3790-070518-3790-170518-3790-270518-3790-370518-3790-4- Official label
- DailyMed (National Library of Medicine), updated Jul 27, 2026
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